تفاعل #2286295

معادلة التفاعل

2-[3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-ethanol

2-[3,5-Dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-ethanol

Jones Reagent

→

[3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-acetic acid

المردود 95.0%

[3,5-Dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-acetic acid

المردود 95.0%

المذيبات

acetone

ظروف التفاعل

المعالجة

1. 1
   أخرىprepared via standard method) slowly dropwise at −4° C
2. 2
   أخرىThe red reaction mixture
3. 3
   أخرىwas quenched with isopropanol
4. 4
   ترشيحThe resulting green suspension was filtered through celite
5. 5
   غسيلthe celite was washed well with ethyl acetate (600 mL)
6. 6
   غسيلThe filtrate was washed with water (600 mL)
7. 7
   أخرىThe organic layer was separated
8. 8
   تجفيفdried with magnesium sulfate
9. 9
   ترشيحfiltered
10. 10
    تركيزconcentrated
11. 11
    أخرىThe resulting solid was dried under vacuum overnight

الإجراء التجريبي

A solution of 2-[3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-ethanol (17) (8.4 g, 23.2 mmol) in acetone (270 mL) was treated with Jones Reagent (34.8 mL of a 2.7 M solution, prepared via standard method) slowly dropwise at −4° C. The resulting red reaction mixture was stirred for 1 h at −3 to 0° C. The red reaction mixture was quenched with isopropanol. The resulting green suspension was filtered through celite and the celite was washed well with ethyl acetate (600 mL). The filtrate was washed with water (600 mL) and a saturated aqueous sodium chloride solution (300 mL). The organic layer was separated, dried with magnesium sulfate, filtered, and concentrated. The resulting solid was dried under vacuum overnight to afford [3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-acetic acid (18) (8.3 g, 95%) as a white solid; LRMS for C15H15Cl3N2O3 (M+) m/z=377. Molecular Weight=377.6574; Exact Mass=376.0148

المصدر